A treatable case of autoimmune GFAP astrocytopathy presenting chronic progressive cognitive impairment

2020 ◽  
Vol 41 (10) ◽  
pp. 2999-3002
Author(s):  
Takahiro Natori ◽  
Kazumasa Shindo ◽  
Akihiro Okumura ◽  
Akio Kimura ◽  
Yoshihisa Takiyama
2022 ◽  
pp. 0957154X2110625
Author(s):  
Carlo Maggini ◽  
Riccardo Dalle Luche

Pre-Kraepelinian observations converged in Kahlbaum’s and Hecker’s description of Hebephrenia. For Kraepelin, Hebephrenia was an ‘idiopathic incurable dementia whose onset is in adolescence’. It became the core of ‘Dementia Praecox’, and then Bleulerian ‘Schizophrenia’. In recent decades, the resurgence of the ‘late neurodevelopment’ hypothesis of schizophrenia has brought into focus Hecker’s clinical reports of adolescents who, as a result of a putative loss of psychic energy, showed a rapidly progressive cognitive impairment leading to functional and behavioural disorganization. This paper summarizes the nineteenth-century conceptualization of Hebephrenia as a developmental illness.


2010 ◽  
Vol 23 (2) ◽  
pp. 333-334
Author(s):  
V M Aziz ◽  
J. Yagoub ◽  
K. Saba ◽  
M. Asaad

Alzheimer's disease (AD) manifests clinically with an insidious onset and slow but progressive cognitive impairment. The clinical picture of AD can be classified into cognitive and behavioral changes. The initial deficit usually manifests as an amnesic syndrome which may progress very gradually for several years before impairment in other cognitive domains, such as language, semantic memory and visuospatial function, becomes apparent (Hodges and Patterson, 1995).


Stroke ◽  
2016 ◽  
Vol 47 (2) ◽  
pp. 577-580 ◽  
Author(s):  
Anand Viswanathan ◽  
Steven M. Greenberg ◽  
Philip Scheltens

Neurosurgery ◽  
1989 ◽  
Vol 25 (6) ◽  
pp. 971-975 ◽  
Author(s):  
Michael K. Morgan ◽  
Thoralf M. Sundt ◽  
Wayne O. Houser

Abstract The management of the case of a 9-year-old boy with progressive cognitive impairment due to arteriovenous fistulae at the apex of the inferior sagittal sinus is reported. This represents a unique location for an extraparenchymal deep central arteriovenous malformation. The patient underwent staged ablation of the lesion by surgery. The postoperative course was complicated by expansion of an aneurysmal vein of Galen undergoing thrombosis and hyperperfusion syndrome, but the patient ultimately made a satisfactory recovery.


Stroke ◽  
2018 ◽  
Vol 49 (Suppl_1) ◽  
Author(s):  
Heba A Ahmed ◽  
Tauheed Ishrat ◽  
Bindu Pillai ◽  
Abdelrahman Y Fouda ◽  
Mohammed A Sayed ◽  
...  

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